Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs55770810
rs55770810
10 0.763 0.280 17 43063931 missense variant G/A;T snv 2.4E-05; 8.0E-06 0.800 0
dbSNP: rs28897672
rs28897672
16 0.732 0.280 17 43106487 missense variant A/C;G;T snv 3.2E-05 0.730 1.000 3 2006 2010
dbSNP: rs1800726
rs1800726
1 1.000 0.120 17 43070993 missense variant C/G;T snv 0.700 0
dbSNP: rs1800751
rs1800751
5 0.851 0.160 17 43047676 missense variant G/A;C snv 4.0E-06 0.700 0
dbSNP: rs1800757
rs1800757
1 1.000 0.120 17 43051069 missense variant G/A snv 0.700 0
dbSNP: rs273900729
rs273900729
2 0.925 0.160 17 43082529 missense variant A/G snv 0.700 0
dbSNP: rs80187739
rs80187739
5 0.851 0.200 17 43067608 missense variant C/A;G;T snv 1.2E-05 0.700 0
dbSNP: rs80356898
rs80356898
11 0.752 0.200 17 43093844 stop gained G/A;C snv 2.8E-05; 4.0E-06 0.700 0
dbSNP: rs80356993
rs80356993
3 0.925 0.120 17 43063937 missense variant A/G;T snv 0.700 0
dbSNP: rs80357233
rs80357233
4 0.882 0.200 17 43093393 stop gained G/C;T snv 4.0E-06 0.700 0
dbSNP: rs80357438
rs80357438
5 0.851 0.200 17 43124032 stop gained A/G;T snv 0.700 0
dbSNP: rs80357462
rs80357462
1 1.000 0.120 17 43057083 missense variant G/A;C snv 0.700 0
dbSNP: rs80357474
rs80357474
5 0.827 0.200 17 43049188 missense variant A/C;G;T snv 8.0E-06 0.700 0
dbSNP: rs80357669
rs80357669
5 0.851 0.200 17 43093074 frameshift variant G/- delins 0.700 0
dbSNP: rs80357828
rs80357828
3 0.882 0.200 17 43092155 frameshift variant GA/- delins 0.700 0
dbSNP: rs1799950
rs1799950
13 0.752 0.240 17 43094464 missense variant T/C snv 4.7E-02 4.6E-02 0.030 1.000 3 1999 2018
dbSNP: rs748876625
rs748876625
10 0.807 0.160 17 43104122 missense variant C/A;G snv 1.2E-05 0.020 1.000 2 2003 2012
dbSNP: rs786203319
rs786203319
6 0.827 0.160 17 43115759 missense variant G/A snv 0.020 0.500 2 2007 2010
dbSNP: rs80357750
rs80357750
8 0.790 0.200 17 43115759 frameshift variant G/- delins 0.020 0.500 2 2007 2010
dbSNP: rs80357796
rs80357796
11 0.752 0.240 17 43094464 frameshift variant T/- del 0.020 1.000 2 1999 2009
dbSNP: rs886039920
rs886039920
7 0.807 0.160 17 43115755 frameshift variant ACAGG/- delins 0.020 0.500 2 2007 2010
dbSNP: rs11655505
rs11655505
8 0.776 0.160 17 43126360 intron variant G/A snv 0.31 0.010 1.000 1 2013 2013
dbSNP: rs1800709
rs1800709
6 0.851 0.160 17 43093010 missense variant G/A snv 1.7E-03 1.4E-03 0.010 1.000 1 1996 1996
dbSNP: rs190900046
rs190900046
5 0.827 0.160 17 43104197 synonymous variant A/C snv 8.0E-06 4.2E-05 0.010 1.000 1 2014 2014
dbSNP: rs28897696
rs28897696
11 0.807 0.200 17 43063903 missense variant G/A;C;T snv 2.8E-05; 4.0E-06; 2.0E-05 0.010 1.000 1 1996 1996